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8/6/2019 SixSteps to Mushroom Farming
1/17
Six Steps to
Mushroom Farming
College of Agricultural Sciences
Agricultural Research and Cooperative Extension
Daniel J. Royse1 and Robert B. Beelman21Professor of Plant Pathology,
2Professor of Food Science, The Pennsylvania State
University, College of Agricultural Sciences, University Park, PA 16803
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why water and supplements are added periodically, and the compost pile is aerated as itmoves through the turner.
Figure 1. Loose straw ready for incorporation into compost windrow (top left); compost
windrow (top right); aerated Phase I compost wharf under roof (note groves in concrete, bottom
left); grove showing aeration nozzle (bottom right, arrow).
The quality of raw materials used to make mushroom compost are highly variable and are
known to influence compost performance in terms of spawn run and mushroom yield.The geographical source of wheat straw, the variety (winter or spring) and the use of
nitrogen fertilizer, plant growth regulators and fungicides may affect compost
productivity. Wheat straw should be stored under cover to minimize growth of unwantedand potentially detrimental fungi and bacteria prior to its use to produce compost.
Gypsum is added to minimize the greasiness compost normally tends to have. Gypsum
increases the flocculation of certain chemicals in the compost, and they adhere to straw or
hay rather than filling the pores (holes) between the straws. A side benefit of this
phenomenon is that air can permeate the pile more readily, and air is essential to thecomposting process. The exclusion of air results in an airless (anaerobic) environment in
which deleterious chemical compounds are formed which detract from the selectivity ofmushroom compost for growing mushrooms. Gypsum is added at the outset of
composting at 40 lb per ton of dry ingredients.
Nitrogen supplements in general use today includes corn distillers grain, seed meals of
soybeans, peanuts, or cotton, and chicken manure, among others. The purpose of these
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supplements is to increase the nitrogen content to 1.5 percent for horse manure or 1.7percent for synthetic, both computed on a dry weight basis. Synthetic compost requires
the addition of ammonium nitrate or urea at the outset of composting to provide the
compost microflora with a readily available form of nitrogen for their growth andreproduction.
The initial compost pile should be 5 to 6 feet wide, 5 to 6 feet high, and as long as
necessary. A two-sided box can be used to form the pile (rick), although some turners areequipped with a "ricker" so a box isnt needed. The sides of the pile should be firm and
dense, yet the center must remain loose throughout Phase I composting. As the straw orhay softens during composting, the materials become less rigid and compactions can
easily occur. If the materials become too compact in the traditional Phase I process, air
cannot move through the pile and an anaerobic environment will develop. The problem ofan anaerobic center core in the compost has largely been overcome by using forced
aeration.
Turning and watering are done at approximately 2-3 day intervals, but not unless the pileis hot (145 to 170F). Turning provides the opportunity to water, aerate, and mix the
ingredients, as well as to relocate the straw or hay from a cooler to a warmer area in the
pile, outside versus inside. Supplements are also added when the compost is turned, but
they should be added early in the composting process. The number of turnings and thetime between turnings depends on the condition of the starting material and the time
necessary for the compost to heat to temperatures above 145F.
Water addition is critical since too much will exclude oxygen by occupying the porespace, and too little can limit the growth of bacteria and fungi. As a general rule, water is
added up to the point of leaching when the pile is formed and at the time of first turning,
and thereafter either none or only a little is added for the duration of composting. On thelast turning before Phase II composting, water can be applied generously so that when the
compost is tightly squeezed, water drips from it. There is a link between water, nutritivevalue, microbial activity, and temperature, and because it is a chain, when one condition
is limiting for one factor, the whole chain will cease to function.
Phase I composting lasts from 6 to 14 days, depending on the nature of the material at thestart and its characteristics at each turn. There is a strong ammonia odor associated with
composting, which is usually complemented by a sweet, moldy smell. When compost
temperatures are 155F and higher, and ammonia is present, chemical changes occurwhich result in a food rather exclusively used by the mushrooms. As a by-product of the
chemical changes, heat is released and the compost temperatures increase. Temperatures
in the compost can reach 170 to 180F during the second and third turnings when adesirable level of biological and chemical activity is occurring. At the end of Phase I thecompost should: a) have a chocolate brown color; b) have soft, pliable straws, c) have a
moisture content of from 68 to 74 percent; and d) have a strong smell of ammonia. When
the moisture, temperature, color, and odor described have been reached, Phase Icomposting is completed.
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2. Phase II: Finishing the Compost
There are two major purposes to Phase II composting. Pasteurization is necessary to kill
any insects, nematodes, pest fungi, or other pests that may be present in the compost. And
second, it is necessary to condition the compost and remove the ammonia that formed
during Phase I composting. Ammonia at the end of Phase II in a concentration higherthan 0.07 percent is often inhibitory to mushroom spawn growth, thus it must be
removed; generally, a person can smell ammonia when the concentration is above 0.10percent.
Phase II takes place in one of three places, depending on the type of production systemused. For the zoned system of growing, compost is packed into wooden trays, the trays
are stacked six to eight high, and are moved into an environmentally controlled Phase II
room. Thereafter, the trays are moved to special rooms, each designed to provide theoptimum environment for each step of the mushroom growing process. With a bed or
shelf system, the compost is placed directly in the beds, which are in the room used for
all steps of the crop culture. The most recently introduced system, the bulk system, is onein which the compost is placed in an insulated tunnel with a perforated floor and
computer-controlled aeration; this is a room specifically designed for Phase II
composting (Fig. 2).
The compost, whether placed in beds, trays, or bulk, should be filled uniformly in depthand density or compression. Compost density should allow for gas exchange, since
ammonia and carbon dioxide will be replaced by outside air.
Figure 2. Phase II tunnels used to pasteurize and condition compost for mushroom production.Left: filling machine in front of closed tunnel, Right: open tunnel ready for filling.
Phase II composting can be viewed as a controlled, temperature-dependent, ecological
process using air to maintain the compost in a temperature range best suited formicroorganisms to grow and reproduce. The growth of these thermophilic (heat-loving)
organisms depends on the availability of usable carbohydrates and nitrogen, some of the
nitrogen in the form of ammonia. These microorganisms produce nutrients or serve as
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nutrients in the compost on which the mushroom mycelium thrives and other organismsdo not.
Completing Phase II in tunnels has become more popular in recent years. Tunnel
composting has the advantage of treating more compost per ft2
compared to more
expensive production rooms. When coupled with bulk spawn run, tunnel compostingoffers the advantage of more uniformity and greater use of mechanization. However,
transfer of the finished compost from the pasteurization tunnel to the bulk spawn runtunnel may increase the risk of infestation of unwanted pathogens and pests compared to
compost that remains in the same room. Thus, higher levels of sanitation may berequired with tunnel composting compared to in-room composting.
It is important to remember the purposes of Phase II when trying to determine the proper
procedure and sequence to follow. One purpose is to remove unwanted ammonia. To thisend the temperature range from 125 to 130F is most efficient since de-ammonifying
organisms grow well in this temperature range. A second purpose of Phase II is to
remove any pests present in the compost by use of a pasteurization sequence.
At the end of Phase II the compost temperature must be lowered to approximately 75 to
80F before spawning (planting) can begin. The nitrogen content of the compost should
be 2.0 to 2.4 percent, and the moisture content between 68 and 72 percent. Also, at the
end of Phase II it is desirable to have 6 to 8 lb of dry compost per square foot of bed ortray surface to obtain profitable mushroom yields. It is important to have both the
compost and the compost temperatures uniform during the Phase II process since it is
desirable to have as homogenous a material as possible.
3. Spawning
As a mushroom matures, it produces millions of microscopic spores on mushroom gillslining the underside of a mushroom cap. These spores function roughly similar to the
seeds of a higher plant. However, growers do not use mushroom spores to seed
mushroom compost because they germinate unpredictably and therefore, are not reliable.Fortunately, mycelium (thin, thread-like cells) can be propagated vegetatively from
germinated spores, allowing spawn makers to multiply the culture for spawn production.
Specialized facilities are required to propagate mycelium, so the mushroom myceliumremains pure. Mycelium propagated vegetatively on various grains or agars is known as
spawn, and commercial mushroom farmers purchase spawn from companies specializing
in its manufacture.
Spawn makers start the spawn-making process by sterilizing a mixture of millet grainplus water and chalk; rye, wheat, and other small grain may be substituted for millet.Sterilized horse manure formed into blocks was used as the growth medium for spawn up
to about 1940, and this was called block or brick spawn, or manure spawn; such spawn is
not used today. Once sterilized grain has a bit of mycelium added to it, the grain andmycelium is shaken 3 times at 4-day intervals over a 14-day period of active mycelial
growth. Once the grain is colonized by the mycelium, the product is called spawn (Fig.
3). Spawn can be refrigerated for a few months, so spawn is made in advance of a
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farmers order for spawn.
Figure 3. Mushroom spawn from open bag (left); close up of millet spawn (right).
Spawn is distributed on the compost and then thoroughly mixed into the compost. Foryears this was done by hand, broadcasting the spawn over the surface of the compost andruffling it in with a small rake-like tool. In recent years, however, for the bed system,
spawn is mixed into the compost by a special spawning machine that mixes the compost
and spawn with tines or small finger-like devices. In a tray or batch system, spawn ismixed into the compost as it moves along a conveyer belt or while falling from a
conveyor into a tray. The spawning rate is expressed as a unit or quart per so many square
feet of bed surface; 1 unit per 5 ft2 is desirable. The rate is sometimes expressed on the
basis of spawn weight versus dry compost weight; a 2 percent spawning rate is desirable.
3.1 Supplementation at spawning
In the early 1960s, yield increases were observed when compost was supplemented with
protein and/or lipid rich materials at spawning, casing and later. Up to a 10% increase in
yield was obtained when small amounts of protein supplements were added to thecompost at spawning. Excessive heating and stimulation of competitor molds in the
compost substantially limited the amount of supplement and corresponding benefit that
could be achieved. It was these limitations that were overcome by the invention of
delayed release supplements for mushroom culture (Carroll and Schisler 1976). Thedisadvantages associated with the supplementation of non-composted nutrients to
mushroom compost at spawning were largely overcome by encapsulating micro-droplets
of vegetable oil within a protein coat that was denatured with formaldehyde. Increases ofas much as 60% were obtained. Today, several commercial supplements are available
that can be used at spawning or at casing to stimulate mushroom yield.
Amendment of mushroom substrate with Micromax is another potential opportunity forgrowers to improve the yield capacity of their Phase II compost. Micromax contains a
mixture of nine micronutrients including (percentage dry wt basis): Ca (12%), Mg (3%),
S (12%), B (0.1%), Cu (1%), Fe (17%), Mn (2.5%), Mo (0.05%), Zn (1%), and inertingredients (57.35%). Research has shown that approximately 70% of the yield increase
observed is due to Mn. Commercial supplement makers have begun to add Mn to their
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delayed release nutrients for mushroom culture.
Once the spawn and supplement have been mixed throughout the compost and the
compost worked so the surface is level, the compost temperature is maintained at 75-
80F and the relative humidity is kept high to minimize drying of the compost surface or
the spawn. Under these conditions the spawn will grow - producing a thread-like networkof mycelium throughout the compost. The mycelium grows in all directions from a spawn
grain, and eventually the mycelium from the different spawn grains fuses together,making a spawned bed of compost one biological entity. The spawn appears as a white to
blue-white mass throughout the compost after fusion has occurred. As the spawn grows itgenerates heat, and if the compost temperature increases to above 80 to 85F, depending
on the cultivar, the heat may kill or damage the mycelium and eliminate the possibility of
maximum crop productivity and/or mushroom quality. At temperatures below 74F,spawn growth is slowed and the time interval between spawning and harvesting is
extended.
3.2 Phase III and Phase IV compost
Phase III compost is Phase II compost spawn run in bulk in a tunnel, and ready for casing
when removed from the tunnel and delivered to the grower. If the Phase III compost then
is cased and the spawn allowed to colonize the casing layer before sending to the growing
unit or delivering to growers, it is called Phase IV compost. The successes of both PhaseIII and Phase IV compost depend, to a large extent, on the quality of Phase I and Phase II
composts. Use of Phase III compost may also improve mushroom quality, as
fragmentation of the colonized compost tends to improve initial color and mushroomshelf life. In recent years, the use of bulk Phase III compost has increased in popularity
because it allows an increase in the number of crops a grower can expect from his
production rooms. Phase II production on shelves allows an average of about 4.1 cropsper year whereas growers using Phase III bulk spawn run compost averages about 7.1
crops per year. An additional gain can be made in the number of crops (10-12 crops peryear) when Phase IV is used (Dewhurst 2002; Lemmers 2003; Chang 2006).
3.3 Mushroom varieties
In the United States, mushroom growers use three major mushroom cultivars: a) Smoothwhite hybrid cap smooth, cap and stalk white; b) Off-white hybrid cap scaly with
stalk and cap white; and c) Brown cap smooth, cap chocolate brown with a white stalk.
Within each of the three major groups, there are various isolates, so a grower may have achoice of up to eight strains within each variety. Generally, white and off-white hybrid
cultivars are used for processed foods like soups and sauces, but all isolates are goodeating as fresh mushrooms. In recent years, the brown varieties have gained market share
among consumers. The Crimini variety is similar in appearance to the white mushroomexcept it is brown and has a richer and earthier flavor. The Portobello variety is a large,
open, brown-colored mushroom that can have caps up to 6 inches in diameter. The
Portobello offers a rich flavor and meaty texture.
The time needed for spawn to colonize the compost depends on the spawning rate and its
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distribution, the compost moisture and temperature, compost supplementation, and thenature or quality of the compost. Complete spawn run usually requires 13 to 20 days.
Once the compost is fully-grown with spawn, the next step in production is at hand.
4. Casing
Casing is a top-dressing applied to the spawn-run compost on which the mushrooms
eventually form. A mixture of peat moss with ground limestone can be used as casing.Casing does not need nutrients since casing acts as a water reservoir and a place where
rhizomorphs form. Rhizomorphs look like thick strings and form when the very fine
mycelium fuses together. Mushroom initials, primordia, or pins form on the rhizomorphs,so without rhizomorphs there will be no mushrooms. Casing should be able to hold
moisture since moisture is essential for the development of a firm mushroom. The most
important functions of the casing layer are supplying water to the mycelium for growthand development, protecting the compost from drying, providing support for the
developing mushrooms and resisting structural breakdown following repeated watering.
Supplying as much water as possible to the casing as early as possible without leachinginto the underlying compost provides the greatest yield potential.
Sphagnum peat moss is the most commonly used material for casing. Sphagnum can
range from brown (young, less decomposed, loose textured, surface peat) to black
(compact, more decomposed, deep dug) and may be processed differently at the harvestsite. Milled peat is partially dried before packaging and transport while wet-dug peat is
transported in a saturated form. Some growers prefer wet-dug peat because of the higher
water holding capacity compared to milled peat.
Peat moss-based casing does not require pasteurization because the material is free from
pathogens, weed molds and nematodes that may reduce mushroom yield. One 6-ft3
compressed bale when mixed with water and 40 lb of limestone will cover about 125 ft2of compost surface at about 2 inches depth.
4.1 Casing inoculum (CI)
Casing inoculum is a sterilized mixture of peat, vermiculite and wheat bran that has beencolonized by mushroom mycelium. It is mixed with casing to decrease cropping cycle
time, improve uniformity of mushroom distribution over the bed and improve mushroom
cleanliness. Mycelium from the CI colonizes the casing layer while it fuses with the
underlying mycelium of the compost. This allows more breaks per crop or more cropsper year.
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Figure 4. Casing inoculum used to inoculate casing for more rapid mycelial colonization.
4.2 Supplementation at casing
The addition of nutrients at casing was first tried in the early 1960s. Results showed that
much greater amounts of nutrients could be added at casing than at spawning and thatyield increases were almost proportional to the amount added. Although yield increases
as high as 100% may be realized, certain potential problems and limitations exist for
supplementation at casing. Weed molds, nematodes and pathogens must not be present
in the compost when supplementing at casing. These organisms will be dispersedthroughout the compost when it is fragmented prior to supplementation and can multiply
very rapidly before the mushroom mycelium recovers its growth.
Managing the crop after casing requires that the compost temperature be kept at around75F for up to 5 days after casing, and the relative humidity should be high. Thereafter,
the compost temperature should be lowered about 2F each day until small mushroominitials (pins) have formed. Throughout the period following casing, water must be
applied intermittently to raise the moisture level to field capacity before the mushroom
pins form. Knowing when, how, and how much water to apply to casing is an "art form"which readily separates experienced growers from beginners.
5. Pinning
Mushroom initials develop after rhizomorphs have formed in the casing. The initials areextremely small but can be seen as outgrowths on a rhizomorph. Once an initial
quadruples in size, the structure is a pin. Pins continue to expand and grow larger through
the button stage, and ultimately a button enlarges to a mushroom (Fig. 5). Harvestablemushrooms appear 18 to 21 days after casing. Pins develop when the carbon dioxide
content of room air is lowered to 0.08 percent or lower, depending on the cultivar, by
introducing fresh air into the growing room. Outside air has a carbon dioxide content of
about 0.04 percent.
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Figure 5. Mushrooms forming and maturing on the casing a 2-inch layer of neutralized peat.
Both pins and young mushrooms are visible.
The timing of fresh air introduction is very important and is something learned only
through experience. Generally, it is best to ventilate as little as possible until the
mycelium has begun to show at the surface of the casing, and to stop watering at the timewhen pin initials are forming. If the carbon dioxide is lowered too early by airing too
soon, the mycelium will stop growing through the casing and mushroom initials formbelow the surface of the casing. As such mushrooms continue to grow, they push through
the casing and are dirty at harvest time. Too little moisture can also result in mushrooms
forming below the surface of the casing. Pinning affects both the potential yield andquality of a crop and is a significant step in the production cycle.
6. Cropping
The terms flush, break, or bloom are names given to the repeating 3- to 5-day harvestperiods during the cropping cycle; these are followed by a few days when no mushrooms
are available to harvest. This cycle repeats itself in a rhythmic fashion, and harvesting can
go on as long as mushrooms continue to mature. Most mushroom farmers harvest for 35to 42 days, although some harvest a crop for 60 days, and harvest can go on for as long as
150 days.
Air temperature during cropping should be held between 57 to 62F for good results.
This temperature range not only favors mushroom growth, but cooler temperatures can
lengthen the life cycles of both disease pathogens and insects pests. It may seem odd thatthere are pests that can damage mushrooms, but no crop is grown that does not have to
compete with other organisms. Mushroom pests can cause total crop failures, and often
the deciding factor on how long to harvest a crop is based on the level of pest infestation.
These pathogens and insects can be controlled by cultural practices coupled with the useof pesticides, but it is most desirable to exclude these organisms from the growing rooms.
The relative humidity in the growing rooms should be high enough to minimize the
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drying of casing but not so high as to cause the cap surfaces of developing mushrooms tobe clammy or sticky. Water is applied to the casing so water stress does not hinder the
developing mushrooms; in commercial practice this means watering 2 to 3 times each
week. Each watering may consist of more or fewer gallons, depending on the dryness ofthe casing, the cultivar being grown, and the stage of development of the pins, buttons, or
mushrooms. Most first-time growers apply too much water and the surface of the casingseals; this is seen as a loss of texture at the surface of the casing. Sealed casing preventsthe exchange of gases essential for mushroom pin formation. One can estimate how much
water to add after first break has been harvested by realizing that 90 percent of the
mushroom is water and a gallon of water weighs 8.3 lb. If 100 lb of mushrooms were
harvested, 90 lb of water (11 gal.) were removed from the casing; and this is what mustbe replaced before second break mushrooms develop.
Outside air is used to control both the air and compost temperatures during the harvest
period. Outside air also displaces the carbon dioxide given off by the growing mycelium.
The more mycelial growth, the more carbon dioxide produced, and since more growth
occurs early in the crop, more fresh air is needed during the first two breaks. The amountof fresh air also depends on the growing mushrooms, the area of the producing surface,
the amount of compost in the growing room, and the condition or composition of the
fresh air being introduced. Experience seems to be the best guide regarding the volume ofair required, but there is a rule of thumb: 0.3ft/ft2/hr when the compost is 8 inches deep,
and of this volume 50 to 100 percent must be outside air.
Ventilation is essential for mushroom growing, and it is also necessary to controlhumidity and temperature. Moisture can be added to the air by a cold mist or by live
steam, or simply by wetting the walls and floors. Moisture can be removed from the
growing room by: 1) admitting a greater volume of outside air; 2) introducing drier air; 3)moving the same amount of outside air and heating it to a higher temperature since
warmer air holds more moisture and thus lowers the relative humidity. Temperature
control in a mushroom growing room is no different from temperature control in your
home. Heat can originate from hot water circulated through pipes mounted on the walls.Hot, forced air can be blown through a ventilation duct, which is rather common at more
recently built mushroom farms. There are a few mushroom farms located in limestone
caves where the rock acts as both a heating and cooling surface depending on the time ofyear. Caves of any sort are not necessarily suited for mushroom growing, and abandoned
coalmines have too many intrinsic problems to be considered as viable sites for a
mushroom farm. Even limestone caves require extensive renovation and improvementbefore they are suitable for mushroom growing, and only the growing occurs in the cave
with composting taking place above ground on a wharf.
Mushrooms are harvested in a 7- to 10-day cycle, but this may be longer or shorter
depending on the temperature, humidity, cultivar, and the stage when they are picked
(Fig. 6). When mature mushrooms are picked, an inhibitor to mushroom development isremoved and the next flush moves toward maturity. Mushrooms are normally picked at a
time when the veil is not too far extended. Consumers in North America want closed,
tight, and white or brown (Crimini) mushrooms while open browns (Portobello) arepreferred by some consumers. The maturity of a mushroom is assessed by how far the
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veil is stretched, and not by how large the mushroom is. Consequently, maturemushrooms are both large and small, although farmers and consumers alike prefer
medium- to large-size mushrooms.
Figure 6. Harvesting of mushrooms. Each mushroom is hand harvested, the base of the
mushroom is trimmed, and the clean, mature mushroom placed in a basket.
Picking and packaging methods often vary from farm to farm. Freshly harvested
mushrooms must be kept refrigerated at 35 to 45F. To prolong the shelf life of
mushrooms, it is important that mushrooms "breathe" after harvest, so storage in a non-
waxed paper bag is preferred to a plastic bag.
A question frequently arises concerning the need for illumination while the mushrooms
grow. Mushrooms do not require light to grow; only green plants require light for
photosynthesis. However, growing rooms can be illuminated to facilitate harvesting orcropping practices.
Nutrients. Mushrooms are a good source of numerous nutrients. Data presented in Figure7 demonstrate this with Crimini mushrooms. They are an excellent source (contain over
20% of the RDA in a serving) of selenium, riboflavin (vitamin B2) and copper and are a
good source (contain over 10% of RDA) for niacin (vitamin B3), pantothenic acid(vitamin B5) and potassium. Criminis also contain rich amounts of thiamin (Vitamin
B1), zinc, vitamin B6, protein, folic acid, fiber, manganese and magnesium. On the other
hand, mushrooms are low in fat, sodium and calories.
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Nutrients in Crimini Mushrooms, Raw
0.1
2
2
2
3
4
5
6
7
11
13
16
20
24
31
0 10 20 30 40
sodium
manganese
magnesium
dietary fiber
folate
protein
vitamin B6
zinc
vitamin B1
potassium
vitamin B5
vitamin B3
copper
vitamin B2
selenium
3
oz-w
t(84
g)
% Daily Value
Excellent source
(>20% RDA)
Good source
(>10% RDA)
Rich in
Very low amount
Figure 7. Nutrients in crimini mushrooms based on FDA reference serving size of 84 g for raw
mushrooms. Mushrooms are not a significant source of saturated fat, trans fat, cholesterol,
sugars, vitamin A and calcium. Source: Mushroom Council.
Vitamin D. Recent research has shown that when UV light is shined on mushrooms,there is a major boost in the vitamin D2 content of the mushrooms. A single serving ofmushrooms will contain over 800% of the recommended daily allowance (RDA) of
vitamin D2 once exposed to just five minutes of UV light after being harvested. This may
be a convenient way for people who do not eat fish or drink milk to obtain their dailyrequirement of vitamin D.
Dietary fiber (DF). Mushrooms contain numerous complex carbohydrates includingpolysaccharides such as glucans and glycogen, monosaccharides, disaccharides, sugar
alcohols and chitin. Most polysaccharides are structural components of the cell walls
(chitin and glucans) and are indigestible by humans; thus they may be considered as
dietary fiber. Dietary fiber may help to prevent many diseases prevalent in affluentsocieties. Portobello mushrooms contain a higher level of DF than the white variety of
mushrooms.
Selenium. A serving (3 ounces) of Crimini mushrooms provides almost one-third of the
RDA for selenium, according to the USDA National Nutrient Database. Selenium hasbeen shown to decrease prostate cancer by more than 60% according to findings from the
Baltimore Longitudinal Study on Aging. Men with the lowest blood selenium levels
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were 4-5 times more likely to have prostate cancer than those with the highest seleniumlevels and that selenium levels tend to decrease with age.
Selenium levels can be reliably increased in mushrooms by adding sodium selenite to
mushroom compost. Some commercial supplement makers are now adding this
compound to their delayed release nutrients for mushroom culture.
Potassium. Crimini mushrooms are a good source of potassium, an element that isimportant in the regulation of blood pressure, maintenance of water in fat and muscle,
and to ensure the proper functioning of cells. A 3-ounce Portobello contains more
potassium than a banana or an orange. To date, attempts to enhance the potassiumcontent of mushrooms have met with only limited success.
Antioxidants. Portobello and Crimini mushrooms are good sources of antioxidants and
rank with carrots, green beans, red peppers and broccoli as good sources of dietaryantioxidants. They are rich sources of polyphenols that are the primary antioxidants in
vegetables and are the best source of L-ergothioneine (ERGO) a potent antioxidant only
produced in nature by fungi. Crimini mushrooms contain over 15 times more ERGOthan the previously best-known dietary sources of ERGO.
Environmental Concerns
Odors. Nuisance complaints, a result of mushroom compost preparation in close
proximity to residential areas, are a problem for some mushroom farms. Offensive odors
associated with the preparation of mushroom compost are the primary reasons for thesecomplaints. A combination of suburbanization and the heightened sensitivity of the
general population to environmental issues have focused public attention on this issue.
Growers have adopted several measures to reduce the environmental impact of
mushroom farming, including the practice of forced aeration of Phase I compostcontained in bunkers or tunnels. However, the issue of offensive odor generation
continues to place pressure on mushroom growers.
Disposal of post-crop mushroom compost. After the last flush of mushrooms has been
picked, the growing room should be closed off and the room pasteurized with steam. This
final pasteurization is designed to destroy any pests that may be present in the crop or thewoodwork in the growing room, thus minimizing the likelihood of infesting the next
crop.
Post-crop mushroom compost (MC) is the material left over after the crop has been
terminated (Fig. 8). It has many uses and is a valued product in the horticultural industry.One of the major uses of MC is for suppression of artillery fungi in landscape mulch. Theartillery fungi grow rapidly throughout moist landscape mulch, and produce sticky spore
masses about the size of a pinhead. These spores are forcibly discharged toward light
colored surfaces such as house siding and cars. Once the spores dry they are nearlyimpossible to remove without leaving an unsightly brown stain on the surface. The
incorporation of 20-40% MC into mulch effectively suppress the artillery fungi.
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Figure 8. Post-crop mushroom compost (MC) being loaded onto a truck as it is removed from a
mushroom house.
Conclusion
It takes approximately 14 weeks to complete an entire production cycle, from the start of
composting to the final steaming off after harvesting has ended. For this work a
mushroom grower can expect anywhere from 0 to 8 lb per ft2; the national average for
2006 was 5.92 lb per square foot. Final yield depends on how well a grower has
monitored and controlled the temperature, humidity, pests, and so on. All things
considered, the most important factors for good production appear to be experience plusan intuitive feel for the biological rhythms of the commercial mushroom. The production
system used to grow a crop can be chosen after the basics of mushroom growing are
understood.
Related Readings
Beelman, R.B., D.J. Royse, and N. Chikthimmah. 2004. Bioactive components inAgaricus
bisporus of nutritional, medicinal or biological importance. Mushroom Science16:1-16.
Beyer, D.M. 2003. Basic procedures forAgaricus mushroom growing. College of Agricultural
Sciences, The Pennsylvania State University, University Park, PA.
Carroll, A.D. and L.C. Schisler. 1976. Delayed release nutrient supplement for mushroom culture.Applied and Environmental Microbiology 31:499-503.
Chang, S.T. 2006. The world mushroom industry: trends and technological development.
International J. Medicinal Mushrooms 8:297-314.
Davis, D.D., Kuhns, L.J., Harpster, T.L., 2005. Use of mushroom compost to suppress artillery
fungi. J. Environ. Hort. 23 (4), 212-215.
Dewhurst, M. 2002. Phase IIIthe future? Mushroom J. 626:17-18.
Lemmers, G. 2003. The merits of bulk Phase III. Mushroom J. 642:17-22.
8/6/2019 SixSteps to Mushroom Farming
17/17
2nd
Edition
Van Griensven, L.J.LD (Ed.). 1988. The Cultivation of Mushrooms. Mushroom Experimental
Station, Horst, The Netherlands.
Wuest, P.J. and G.D. Bengtson (Eds.). 1982. Penn State Handbook for Commercial Mushroom
Growers. College of Agricultural Sciences, The Pennsylvania State University, University
Park, PA.
Reviewed by:
Dr. Gary W. Moorman, Professor of Plant Pathology, Department of Plant Pathology, The
Pennsylvania State University, University Park, PA 16802.
Dr. Donald D. Davis, Professor of Plant Pathology, Department of Plant Pathology, The
Pennsylvania State University, University Park, PA 16802.